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Acarbose versus trans-chalcone: comparing the effect of two glycosidase inhibitors on obese mice

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1 Department of Biology, Science

and Research Branch, Islamic Azad University, Tehran, Iran

2 Endocrinology and Metabolism

Research Center, Endocrinology and Metabolism Research Institute, Tehran University of Medical Sciences, Tehran, Iran

3 National Nutrition and Food

Science Research Institute, Shahid Beheshti University of Medical Science, Tehran, Iran

4 Biosensor Research Center,

Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran

5 Endocrinology and Metabolism

Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran

Correspondence to:

Parichehreh Yaghmaei Department of Biology, Science and Research Branch, Islamic Azad University,

Hesarak – 1477893855 – Tehran, Iran yaghmaei_p@srbiau.ac.ir

Received on May/16/2014 Accepted on Apr/16/2015

DOI: 10.1590/2359-3997000000038

Acarbose versus

trans-chalcone: comparing the

effect of two glycosidase

inhibitors on obese mice

Fatemeh Jalalvand1, Mahsa M. Amoli2, Parichehreh Yaghmaei1,

Masoud Kimiagar3, Azadeh Ebrahim-Habibi4,5

ABSTRACT

Objective: Acarbose and trans-chalcone are glucosidase inhibitors whose beneficial effects have been demonstrated in diabetes. The present study aimed at investigating their potential effects in obesity. Materials and methods: NMRI male mice (n = 48) were subjected to a high fat diet for four weeks, which induced an initial state of obesity. One control group was given normal rodent diet. Obese animals were then switched to normal rodent diet, and divided to four groups (n = 12 in each): untreated, sham (receiving grape seed oil), and experimental groups receiving acarbose and

trans-chalcone (12 mg/kg) during eight weeks. Body weight, blood glucose and other biochemical

parameters including triglycerides (TG), cholesterol, HDL, AST, and ALT were measured, as well as leptin, adiponectin, TNF-α, and total antioxidant capacity (TAC). Histological studies were performed on adipose cells and liver tissue samples. Results: All factors were affected in a positive manner by acarbose, save for body weight, blood sugar and leptin levels, on which acarbose effects, although observable, were not statistically significant. Grape seed oil, used as a solvent for trans-chalcone was found to possess significant effect on TG and TAC, and had beneficial effects on other factors includ-ing liver enzymes and cholesterol. Trans-chalcone effects were significant on HDL, leptin and ALT. All compounds seemed to be able to affect fat deposition in liver tissue, and decrease the size of adipose tissue cells to some extent. Conclusion: In conclusion, the tested compounds were able to affect lipid accumulation in tissues and influence adipokines, which may result in an enhanced state with regard to inflammation and oxidative stress. Arch Endocrinol Metab. 2015;59(3):202-9

Keywords

Acarbose; chalcone; obesity; adipocyte; adipokine; antioxidant

INTRODUCTION

O

besity is a chronic metabolic disorder related to energy imbalance resulting from a dispropor-tion between food consumpdispropor-tion and physical activity (1). Currently, a high prevalence of obesity is observed worldwide, in both adults and children (2,3). Health practitioners’ concern about obesity prevalence is also due to the fact that this condition is accompanied by a wide range of complications including diabetes, nonal-coholic fatty liver disease (NAFLD) (4).

Among various approaches to combat obesity, inhi-bition of digestive enzymes is a logical solution. Lipase inhibitor orlistat that was used as an anti-obesity drug may cause various side effects including severe liver injury (5), but the search for other lipase inhibitors

continues, and other compounds have been reported as potential drugs (6). Glucosidase enzymes such as alpha-amylase are also considered to be an anti-diabetic and anti-obesity target (7). Alpha-amylase inhibitors have been demonstrated to reduce blood sugar levels and cause weight loss (8).

Acarbose, which is a glucosidase inhibitor minimally absorbed from the gastrointestinal tract (9), has been used as a therapeutic supplement in diabetes, since it controls the postprandial rise in blood glucose levels (10). Acarbose is a competitive inhibitor of alpha-glu-cosidase and has a noncompetitive inhibitory behavior toward alpha-amylase (11). Trans-chalcone structure is a precursor to flavonoids and chalcone compounds and possess a range of therapeutic properties including

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tioxidant, cytotoxic, anticancer, antimicrobial, antipro-tozoal, antiulcer, antihistaminic and anti-inflammatory (12). We had previously observed the alpha-amylase inhibitory effect of trans-chalcone in vitro (13), and its beneficial effect on streptozotocin–induced diabetic mice (14).

In this study, we aimed at evaluating the effect of

trans-chalcone treatment on obese mice, and

compa-ring it with acarbose.

MATERIALS AND METHODS

Animals

Male NMRI mice (six weeks old) weighing 25 ± 5 g were purchased from the Razi Vaccine and Serum In-stitute, Karaj, Iran. Mice were exposed to a 12-h light/ dark cycle, and were housed in standard cages. The animal room was maintained at a constant temperature of 25 °C. After one week of adaptation to the condi-tions, mice were randomly divided into two groups (n = 12 in each group): normal group (receiving standard rodent diet) and obese group (receiving high-fat diet for eight weeks). The high-fat diet was prepared from a mix of 15 g of mouse pellet standard chow, 10 g of roasted ground nut, 10 g of milk chocolate and 5 g of sesame crackers. To ten-fold of these ingredients 20 g roasted sesame was added, resulting into 18 kJ/g ener-gy content. In addition, the obese group was fed 240 g creamy biscuits (3644 kJ) weekly. The normal group was allowed ad libitum access to standard chow, tak-ing a total of 13 kJ/g weekly (15). After eight weeks, all animals were given standard rodent diet, and the obese animals were divided into four groups: sham, obese and two experimental groups. The experimental groups were treated with either acarbose or trans-chal-cone (12 mg/kg/day) by oral gavage for eight weeks. The obese group did not receive any treatment and the sham groups received grape seed oil which was used as trans-chalcone solvent. Mice were weighed weekly during the eight weeks of treatment. At the end of the experiment, the animals were anesthetized and sacri-ficed; blood samples were collected and immediately centrifuged at 1500 g for 10 min at 4 °C. Serums were then collected and stored at 4 °C until further analyzes were made. The experimental protocol was performed in accordance with the international guidelines set out in the Guide for the Care and Use of Laboratory Animals (Institute of Laboratory Animal Resources,

1996) and approved by the Animal Ethics Committee of the Science and Research Branch, Azad University, Tehran.

Biochemical parameters

Serum levels of total cholesterol, triglyceride, HDL, ALT and AST were measured with the use of enzyma-tic methods (Pars Azmoon, Iran). As a complementary test, blood glucose levels were measured by a gluco-meter apparatus (ACCU-CHEK, Germany).

Adipokines, TNF-alpha and total antioxidant capacity (TAC)

Plasma adiponectin‚ TNF-α and leptin concentration were determined by ELISA (respectively R&D Systems, USA; Enzo life Science, USA and ALPCO, USA). Plas-ma total antioxidant capacity (TAC) levels were mea-sured by a colorimetric method (BioVision, USA).

Histological studies

Sample adipose tissue was fixed in formalin. Smear mi-croscopy of adipose tissue were prepared and stained with hematoxylin and eosin (H&E).

Statistical analysis

The data were statistically analyzed by SPSS. With the use of ANOVA and Tukey’s test. Values are reported as mean ± SD and the level of significance considered at p < 0.05.

RESULTS

Body weight and blood glucose

After the second eight weeks of the experiment, weight gain of animals was compared. It was found that the untreated obese group gained more weight compared with the other groups, while this weight gain was the least in the control group (Table 1). Treatment with acarbose and chalcone prevented the excessive weight gain (Table 1), but not significantly. The obese group presented elevated blood glucose levels compared to the control group (Table 2). Upon treatment, mice showed lower levels of blood glucose, although the change was not significant. The sham and chalcone groups presented a similar result while acarbose was slightly less effective.

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Table 2. Effects of acarbose and chalcone treatment on blood glucose (mg/dL). Mean blood glucose of the mice at week 4 (W4) and week 8 (W8) of the

treatment period is reported. Data are reported as mean ± SD values. P-values are shown in separate columns

Groups Blood glucose (mg/dL)week 4 p (W4) Blood glucose (mg/dL)week 8 p (W8)

Control 132 ± 6.50 Obese p = 0.87 Sham p = 0.57 Acarbose p = 0.98 Chalcone p = 0.096 123.50 ± 2.50 Obese p = 0.89 Sham p = 0.94 Acarbose p < 1.000 Chalcone p < 0.98 Obese 149.50 ± .50 Control p = 0.87 Sham p = 0.98 Acarbose p = 0.72 Chalcone p = 0.66 135.50 ± 5.50 Control p = 0.89 Sham p = 0.66 Acarbose p = 0.88 Chalcone p = 0.73 Sham 159.5 ± .50 Control p = 0.57 Obese p = 0.98 Acarbose p = 0.44 Chalcone p = 0.38 112 ± 7 Control p = 0.94 Obese p = 0.66 Acarbose p = 0.97 Chalcone p = 0.99 Acarbose 125.66 ± 6.98 Control p = 0.98 Obese p = 0.72 Sham p = 0.44 Chalcone p = 1,000 121 ± 14.29 Control p = 1.000 Obese p = 0.88 Sham p = 0.97 Chalcone p = 0.99 Chalcone 123.33 ± 20.89 Control p = 0.96 Obese p = 0.66 Sham p = 0.38 Acarbose p = 1.000 116 ± 15.62 Control p = 0.98 Obese p = 0.73 Sham p = 0.99 Acarbose p = 0.99

Table 1. Effects of acarbose and chalcone treatment on body weight (g). Mean body weight of the mice at the week 1 and week 8 of the treatment period.

(Week 1: w1, Week 8: w8). Data are reported as mean ± SD values. P-values are shown in separate columns

Groups Body weight (kg)Week 1 p (W1) Body weight (g)Week 8 p (W8)

Control 37.88 ± .66 Obese p = 0.32 Sham p = 0.54 Acarbose p = 0.070 Chalcone p = 0.64 39.83 ± .75 Obese p = 0.058 Sham p = 0.71 Acarbose p = 0.49 Chalcone p = 0.58 Obese 40.95 ± .46 Control p = 0.32 Sham p = 0.99 Acarbose p = 0.98 Chalcone p = 0.97 44.08 ± .49 Control p = 0.058 Sham p = 0.54 Acarbose p = 0.49 Chalcone p = 0.43 Sham 40.35 ± .37 Control p = 0.54 Obese p = 0.99 Acarbose p = 0.87 Chalcone p = 0.85 41.75 ± .69 Control p = 0.71 Obese p = 0.54 Acarbose p = 1.000 Chalcone p = 1.000 Acarbose 41.65 ± .73 Control p = 0.07 Obese p = 0.98 Sham p = 0.87 Chalcone p = 1 41.96 ± .85 Control p = 0.49 Obese p = 0.49 Sham p = 1.000 Chalcone p = 1.000 Chalcone 41.76 ± 1.28 Control p = 0.064 Obese p = 0.97 Sham p = 0.050 Acarbose p = 1 41.79 ± 1.0 Control p = 0.58 Obese p = 0.43 Sham p = 1.000 Acarbose p = 1.000 Adipokines

In comparison with the control group, the untreated obese mice had decreased serum adiponectin levels and increased leptin levels (Figure 1 A and B). Upon eight-week administration of acarbose and chalcone, a significant increase of adiponectin level was observed for acarbose (p < 0.01), the effect of chalcone was not significant (Figure 1A). On the other hand, treatment

with chalcone had a remarkable lowering effect on leptin concentrations (p < 0.001 compared to the un-treated obese group), while this decrease was not sig-nificant in acarbose group.

ALT and AST

The untreated obese group had increased levels of se-rum AST and ALT compared with the control group

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AL

T (IU/L)

Control Obese Sham Acarbose Chalcone

** * 400 450 350 300 250 200 150 100 50 0

(Figure 2A and B). Upon treatment, although all AST levels were decreased (Figure 2A), the decrease was found to be significant in the acarbose group only (p < 0.01). In the case of ALT, both chalcone and acar-bose groups showed significant decrease (p < 0.05 and p < 0.01 respectively) (Figure 2B).

Lipids

The serum triglyceride (TG) levels of the untreated obese group were found to be significantly higher than those in the control group, while HDL levels were lo-wer and cholesterol levels lo-were also higher, but not sig-nificantly (Figure 3). Acarbose had a significant effect in lowering TG, increasing HDL and lowering choles-terol levels of the treated obese group (Figure 3). Chal-cone had a significant effect on HDL only (Figure 3B). Interestingly, the sham group showed also significantly decreased TG levels, in a similar manner to acarbose, and chalcone effect itself was not significant.

Figure 1. Effect of acarbose and chalcone supplementation on serum

adiponectin (A) and leptin (B) in mice (n = 12 in each group) after eight

weeks of treatment. Data are shown as mean ± SD. ** p < 0.01 compared with the obese group. * p < 0.05 compared with the obese group.

Leptin (pg/mL)

Control Obese Sham

Acarbose Chalcone 0 50 100 150 200 250 300 *** 1 0.9 0.8 ** 0.7 0.6 Adiponectim (ng/mL) 0.5 0.4 0.3 0.2 0.1 0

Control Obese Sham

Acarbose Chalcone

A A

B B

AST (IU/L)

Control Obese Sham Acarbose Chalcone * 400 350 300 250 200 150 100 50 0

Figure 2. Effect of acarbose and chalcone supplementation on the serum

AST (A) and ALT (B) in mice (n = 12 in each group) after eight weeks of

treatment. Data are shown as mean ± SD. ** p < 0.01 compared with the obese group. * p < 0.05 compared with the obese group.

TAC and TNF-α

Total antioxidant capacity was found to be lower in un-treated obese mice, although not significantly (Figure 4A). Acarbose administration increased remarkably the serum TAC while chalcone had no significant effect. The sham group showed also significantly increased TAC (Figure 4A). TNF-α is an inflammatory fac-tor, which was higher in the untreated obese group,

although not significantly (Figure 4B). Acarbose was found to significantly reduce serum TNF-α levels (p < 0.01), while in the chalcone group decrease occurred, but was not significant.

Histological studies

Adipocytes

Hematoxylin-Eosin (H&E) staining of the adipose tis-sues taken from abdominal fat is shown in figure 5. Adi-pocytes larger size is clearly observed in the untreated

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eser ved. A B A C B HDL (mg/dL) 120 * * 100 80 60 40 20 0

Control Obese Sham

Acarbose Chalcone

Cholesterol (mg/dL)

*

Control Obese Sham

Acarbose Chalcone 180 160 140 120 100 80 60 40 20 0

Figure 3. Effect of acarbose and chalcone supplement on serum triglycerides

(TG) (A), HDL (B), and cholesterol (C) in mice (n = 12 in each group) after

eight weeks of treatment. Data are shown as mean ± SD. ** p < 0.01 compared with the obese group. * p < 0.05 compared with the obese group.

TAC (nmol/I) * ** 4.5 4 3.5 3 2.5 2 1.5 1 0.5 0

Control Obese Sham

Acarbose Chalcone

TNF-alpha (pg/mL)

**

0

Control Obese Sham

Acarbose Chalcone 70 60 50 40 30 20 10

Figure 4. Effects of acarbose and chalcone on serum total antioxidant

capacity (TAC) (A) and TNF-α (B) in mice (n = 12 in each group) after eight

weeks of treatment. Data are shown as mean ± SD. ** p < 0.01 compared with the obese group. * p < 0.05 compared with the obese group.

Triglycerides (mg/dL) ** ** 250 200 150 100 50 0

Control Obese Sham Acarbose Chalcone

obese mice (Figure 5B). Interestingly, both acarbose and chalcone are able to influence the adipose tissue, followed by grape seed oil (administered in the sham group). From the slides, it may be inferred that adipose cells were disrupted by acarbose and chalcone.

Hepatocytes

In the liver sections of obese animals, fat droplets and multinucleate cells are observed. Furthermore, disor-dered cell structure is observed when comparing the untreated obese animals tissue with the control group (Figures 6A and 6B). When treated with grape seed oil, chalcone, and acarbose, cell structures become more ordered and the number of two- and multi-nucleated cells is decreased (Figures 6C-6E).

DISCUSSION

Acarbose has been used as supplementary therapeutic in diabetes (10), could be envisaged as a potential anti-obesity compound as other alpha-amylase inhibitors.

Trans-chalcone, on the other hand, is relatively less

studied as it is a basic polyphenolic structure: usually, studies are done on its derivatives (16). However, with regard to its alpha-amylase inhibitory effect (13), we thought it interesting to be compared with the well-known acarbose.

The high fat diet which was used here induced an initial state of obesity in mice. After that, all mice were fed normal rodent diet, so the compounds effects that we have observed are in fact additional to a switch to a normal diet. In some instances, the grape seed oil that had been used as trans-chalcone solvent has a more pronounced effect than chalcone itself. Grape seed oil has been indeed reported to have beneficial effect in overweight and obese patients (17). Concerning wei-ght loss, acarbose, grape seed oil and trans-chalcone treated groups were all showing a more moderate

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crease in weight gain, compared with the untreated group. With regard to the fact that the control group was also gaining weight, this effect could be interpreted as some weight loss. In this case, trans-chalcone may have not been effective, since its effect was similar to grape seed oil.

While an obvious effect of treatment with high-fat diet and the resulting obesity is an altered lipid profile, the potential of compounds in restoring normal values would be of interest. Acarbose was successful with re-gard to TG and cholesterol levels, while grape seed oil was effective regarding TG and chalcone itself had an effect on HDL levels. Acarbose has been reported to possess beneficial effects on the lipid profile of type 2 diabetes patients (18), and to be able to decrease TG in obese patients with hypertension (with no effect on LDL and HDL) (19). Grape seed oil has been observed to have an effect on decreasing the fat content of other animals bodies (lambs) (20). While more studies are necessary to clarify the exact mechanism of action, we could hypothesize these effects to be related to pheno-lic compounds that are present in grape seed oil (21). Polyphenolic compounds that are structurally related to chalcone, including flavonoids (22) and coumarin chal-cones (23) have been reported to improve lipid profile in high-fat fed or hyperlipidemic animals. Interestingly, the used compounds are also able to act directly on the adipose cells, which presented altered morphology in the treated animals, and chalcone itself seems to

pos-sess an independent effect (i.e, independent from grape seed oil).

Levels of the adipokines leptin and adiponectin, which are considered to be therapeutic targets/tools in obesity (24), were also observed to be affected by these compounds. In our study, acarbose was found to increase adiponectin levels in the treated obese rats, which is in accordance with previous reports concer-ning diabetic patients (25) and diabetic obese rats (26). In our study, leptin levels were not significantly affected by acarbose, which is in contrast with the previously mentioned reports, but it should be noted that in both reports, acarbose had been chronically administered for three months, while our treatment period was ei-ght weeks. The effect of acarbose on adipokines may be linked with its ability to increase insulin sensitivity (27). On the other hand, we have observed a lowering effect of chalcone on leptin levels, which does not seem to have been reported yet for the chalcone core itself, but some flavonoids have been observed to affect adi-pokines, via a pathway which may be dependent (28) or independent (29) to PPARg. There is also a study performed on naringenin chalcone (composed of a fla-vonoid and the chalcone moiety), which indicates that this compound induces adiponectin secretion again via PPARg activation (30).

Overall, these results are indicative of a beneficial effect of the tested compounds on body fat at seve-ral levels, which is also seen in liver cells. Fatty liver is

Figure 5. Effect of acarbose and chalcone on adipose tissue: representative H&E stained sections of perinephric adipose tissue from (A) control group,

(B) obese group, (C) acarbose group, (D) chalcone group and (E) sham group after at eight weeks of treatment.

Figure 6. Effect of acarbose and chalcone on liver tissue representative H&E stained sections of liver tissue from (A) control group, (B) obese group,

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present in obese patients and may lead to toxicity and complications (31). As a consequence to obesity and the subsequent liver disorder, ALT and AST levels may become elevated (32), and these two factors are even considered as supplementary risk factors for metabolic syndrome that could be detected from childhood (33). Both acarbose and chalcone influenced the levels of ALT in a significant manner, and their beneficial effect is also observable on liver tissue. There is also an asso-ciation between adipokine levels and the occurrence of fatty liver and elevated ALT levels (34).

Since obesity is accompanied with an inflammatory state (and increase of inflammatory cytokines) (35), the reduction of these factors by potential anti-obesity compounds could be an indicator of their efficacy in controlling the multiple manifestations of the dise-ase. In our study, obese rats showed increased levels of TNF-alpha, while all tested compounds resulted in some degree of TNF-alpha decrease, but only acarbose effect was significant. It may also be noted that the-se could be indirect effects of the compounds, since adipokines leptin and adiponectin may also influence TNF-alpha levels (36). The inflammatory process that occurs in obesity is also associated with oxidative stress, which is now considered to be a common factor be-tween obesity, diabetes and breast cancer (37). In our study, obese rats showed a moderate decrease in the antioxidant capacity, while acarbose and grape seed oil were able to increase the antioxidant capacity in a significant manner, and chalcone effect is moderate. Polyphenols could prevent the oxidative damage that occurs as a consequence of high fat diet (38). Concer-ning acarbose, a study conducted on diabetic patients has not found any beneficial effect of acarbose on oxi-dative stress (39), while another study suggests a possi-ble capability of acarbose in reducing oxidative stress by increasing hydrogen production in the digestive tract (40).

In conclusion, our study has demonstrated that acarbose has a beneficial effect on the adverse effects of obesity, and a moderate effect on weight. Previous reports on acarbose are mostly related to its use in dia-betes or obesity cases in which diabetic state is present. Since acarbose is observed to affect adipose tissue, li-pid levels, adipokines, and liver enzymes in a relatively limited time period, it may be possible to elicit a bet-ter response upon its use over more than two months. Chalcone, which has a basic polyphenolic structure, is also shown to have an effect on HDL, leptin, adipose

tissue and ALT. It could be suggested that chalcone derivatives may thus be potentially effective candidates in obesity treatment. Finally, the marked effect of grape seed oil in attenuation of obesity consequences is of interest and is worth being more investigated.

Acknowledgments: this study has been partially supported by the Endocrinology and Metabolism Research Institute of Tehran University of Medical Sciences.

Disclosure: no potential conflict of interest relevant to this article was reported.

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